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CCTGATCTTAGAGGGATGTTCAATT[C/T]GCACCTCAAAGTTTAGAAGGCATCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614517 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ARNTL2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
ARNTL2 - aryl hydrocarbon receptor nuclear translocator like 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001248002.1 | Intron | NP_001234931.1 | ||||
NM_001248003.1 | Intron | NP_001234932.1 | ||||
NM_001248004.1 | Intron | NP_001234933.1 | ||||
NM_001248005.1 | Intron | NP_001234934.1 | ||||
NM_020183.4 | Intron | NP_064568.3 | ||||
XM_006719112.3 | Intron | XP_006719175.1 | ||||
XM_006719114.3 | Intron | XP_006719177.1 | ||||
XM_011520766.2 | Intron | XP_011519068.1 | ||||
XM_011520768.2 | Intron | XP_011519070.1 | ||||
XM_011520769.2 | Intron | XP_011519071.1 | ||||
XM_011520770.2 | Intron | XP_011519072.1 | ||||
XM_011520771.2 | Intron | XP_011519073.1 | ||||
XM_017019666.1 | Intron | XP_016875155.1 | ||||
XM_017019667.1 | Intron | XP_016875156.1 | ||||
XM_017019668.1 | Intron | XP_016875157.1 | ||||
XM_017019669.1 | Intron | XP_016875158.1 |